Reaction of N-cyclohexyl-2-(2-hydroxynaphthalen-1-yl)pyrrolidine-1-carboxamide with resorcinol and its derivatives and synthesis of polyphenols
- Авторы: Smolobochkin A.V.1, Gazizov A.S.1, Burilov A.R.1, Pudovik M.A.1
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Учреждения:
- A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
- Выпуск: Том 65, № 5 (2016)
- Страницы: 1377-1379
- Раздел: Brief Communications
- URL: https://journals.rcsi.science/1066-5285/article/view/238354
- DOI: https://doi.org/10.1007/s11172-016-1465-1
- ID: 238354
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Аннотация
An acid-catalyzed pyrrolidine ring opening in 2-(2-hydroxynaphthalen-1-yl)pyrrolidine-1-carboxamides in the presence of resorcinols furnished new calix[4]resorcinols or 1,1-diarylbutanes modified with urea fragments. The process follows the retro-Mannich reaction mechanism, with the 2-naphthol fragment playing the role of the leaving group.
Об авторах
A. Smolobochkin
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Россия, 8 ul. Akad. Arbuzova, Kazan, 420088
A. Gazizov
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Автор, ответственный за переписку.
Email: agazizov@iopc.ru
Россия, 8 ul. Akad. Arbuzova, Kazan, 420088
A. Burilov
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Россия, 8 ul. Akad. Arbuzova, Kazan, 420088
M. Pudovik
A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Center of the Russian Academy of Sciences
Email: agazizov@iopc.ru
Россия, 8 ul. Akad. Arbuzova, Kazan, 420088
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